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(R)-(-)-(2-Octyl)-(p-tolyl)-sulfid, also known as (R)-2-(4-methylphenyl)sulfanyloctane, is a chiral organic compound characterized by its unique molecular structure. It consists of an octyl chain (C8H17) attached to a p-tolyl group (4-methylphenyl) through a sulfur atom, forming a sulfide linkage. (R)-(-)-(2-Octyl)-(p-tolyl)-sulfid is a specific enantiomer, with the "R" configuration indicating its spatial arrangement. It is used in various applications, including as a chiral ligand in asymmetric synthesis and as a building block for more complex molecules. Due to its chirality, it exhibits different physical and chemical properties compared to its mirror image enantiomer, which is crucial in fields such as pharmaceuticals and agrochemicals where the biological activity of compounds can be highly dependent on their stereochemistry.

1517-86-8

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1517-86-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1517-86-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,5,1 and 7 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1517-86:
(6*1)+(5*5)+(4*1)+(3*7)+(2*8)+(1*6)=78
78 % 10 = 8
So 1517-86-8 is a valid CAS Registry Number.

1517-86-8Downstream Products

1517-86-8Relevant academic research and scientific papers

Nickel-Catalyzed Enantioconvergent Reductive Hydroalkylation of Olefins with α-Heteroatom Phosphorus or Sulfur Alkyl Electrophiles

Fu, Yao,He, Shi-Jiang,Li, Yan,Lu, Xi,Wang, Jia-Wang,Wang, Xiao-Xu,Xu, Zhe-Yuan

supporting information, (2020/01/22)

Substantial advances in enantioconvergent C(sp3)-C(sp3) bond formation reactions have been made in recent years through the use of transition-metal-catalyzed cross-coupling reactions of racemic secondary alkyl electrophiles with organometallic reagents. Herein, we report a general process for the asymmetric construction of alkyl-alkyl bonds adjacent to heteroatoms, namely, a nickel-catalyzed enantioconvergent reductive hydroalkylation of olefins with α-heteroatom phosphorus or sulfur alkyl electrophiles. Including the use of readily available olefins, this reaction has considerable advantages, such as mild reaction conditions, a broad substrate scope, and good functional group compatibility, making it a desirable alternative to traditional electrophile-nucleophile cross-coupling reactions.

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